{{Rsnum
|rsid=7734985
|Chromosome=5
|position=96092980
|Orientation=plus
|GMAF=0.3972
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CTD-2337A12.1
|Gene_s=CTD-2337A12.1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.8 | 47.7 | 18.5
| HCB | 33.3 | 40.0 | 26.7
| JPT | 14.3 | 38.1 | 47.6
| YRI | 37.7 | 44.3 | 18.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 33.3 | 40.0 | 26.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=G
  |Pval=2E-6
  |OR=.16
  |ORtxt=[0.093-0.221] unit decrease
  |OA=1
}}

{{on chip | FTDNA}}